Can a shared mentalizing approach reach youths who slip through the cracks?
NCT ID NCT06886165
First seen Sep 18, 2026 · Last updated Sep 18, 2026
Summary
Researchers in Denmark are testing whether a cross-sector support program called My Avenue to HelP (MAP) can be delivered as intended for youths aged 12 to 17 with multiple social and psychological problems. MAP uses principles from Adaptive Mentalization-Based Integrative Treatment (AMBIT) and assigns each young person a key worker and a mentalizing case manager who work with the existing network of schools, social services, and mental health care. The study enrolls 40 youths to receive the one-year intervention and compares them with 20 youths who receive usual management. The trial measures whether families agree to take part, whether staff can maintain regular contact, and how satisfied participants and professionals are with the approach.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Adaptive Mentalization-Based Integrative Treatment (AMBIT), a team-based approach to coordinating care across services
- What this could lead to
- If the approach proves feasible, it could give mental health and social services a practical model for coordinating care around vulnerable youths. That may help young people stay engaged with support and build lasting changes.
- What could go wrong
- This is a small feasibility study, not a test of whether the approach actually improves outcomes. The trial may show that recruitment, retention, or cross-sector collaboration is too difficult to carry out at scale, and any benefits may not hold beyond the study period.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 60 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Mar 2025
- Expected to finish
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Jan 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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12 to 17 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Criterium A) Documented record of multiple problems defined as at least 2 of the following: (i) Absence from school / non-adherence to education (ii) Risk behaviors like alcohol or cannabis abuse, or repeated suicide attempts or self-harm requiring somatic treatment.(iii) Repeated visits at emergency-, trauma-, or acute wards. And/or one of the following: (iv) Contact with police or legal justice system. (v) Homelessness within the last year. * Criterium B) Age 12-17 years at time of inclusion. * Criterium C) Strong indication of mental disorders defined as a diagnosis of a mental disorder. The type of mental disorders will be further substantiated using the DAWBA after recruitment (Goodman et al., 2000). * Criterium D) Written/signed informed consent from all legal guardians (in most cases both parents) and oral consent from youths aged 15 years and older. Written/signed informed consent from the youths themselves will be collected when they turn 18 if they do so during the study period. Exclusion Criteria: * Indications of substantial intellectual disability corresponding to IQ below 50, or a level of daily and social functions that do not enable participation in research (e.g., if the young person is not deemed to have the capacity to understand the implications of the study and provide oral consent). * Not living in Region Zealand.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Child and Adolescent Psychiatric Department, Psychiatry Region Zealand
RECRUITINGRoskilde, Region Sjælland, 4000, Denmark
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